Bayticol 1% is a ready to use pour-on solution used for the treatment and control of biting lice, sucking lice, ticks and mange in cattle. Bayticol 1% is highly effective against red water tick.
Active Ingredient: Flumethrin
Target Species: Cattle
Treats and Controls: Sucking lice, biting lice, mange and ticks
Administration Method: Pour On
Withdrawal Time: 5 days for cattle intended for meat and offal, 10 days for cattle producing milk for human consumption.
Dosage for cattle: 1 ml per 10 kg of bodyweight if dosing for ticks and biting lice or 2 ml per 10 kg bodyweight if dosing for sucking lice and mange.
| Body Weight | Tick and Biting Lice Dose Volume | Number of doses per pack | Sucking Lice and Mange Dose Volume |
| 1 Litre | |||
| 50kg | 5 ml | 200 | 10 ml |
| 100kg | 10 ml | 100 | 20 ml |
| 150kg | 15 ml | 67 | 30 ml |
| 200kg | 20 ml | 50 | 40 ml |
| 250kg | 25 ml | 40 | 50 ml |
| 300kg | 30 ml | 33 | 60 ml |
| 350kg | 35 ml | 29 | 70 ml |
| 400kg | 40 ml | 25 | 80 ml |
| 450kg | 45 ml | 22 | 90 ml |
| 500kg | 50 ml | 20 | 100 ml |
| 550kg | 55 ml | 18 | 110 ml |
| 600kg | 60 ml | 16 | 120ml |
Always read the label and all enclosed information for Bayticol 1% Pour-on before administering to animals!
This Product is only licensed for sale in the Republic of Ireland
Click here to Download Data Sheet
Summary of Product Characteristics
1 NAME OF THE VETERINARY MEDICINAL PRODUCT
Bayticol 10 mg/ml Pour-On Solution
2 QUALITATIVE AND QUANTITATIVE COMPOSITION
Each ml contains:
Active Substance
Flumethrin 10 mg
For a full list of excipients see section 6.1.
3 PHARMACEUTICAL FORM
Pour-on solution.
4 CLINICAL PARTICULARS
4.1 Target Species
Cattle
4.2 Indications for use, specifying the target species
For the control of ticks (Ixodes ricinus), biting lice (Damalinia bovis) and sucking lice (Linognathus vituli,
Haemotopinus eurysternus) and psoroptic mange in cattle.
4.3 Contraindications
None.
4.4 Special warnings for each target species
None.
4.5 Special precautions for use
Special precaution(s) for use in animals:
None.
Special precautions to be taken by the person administering the veterinary medicinal product to animals:
Avoid contact with the skin and eyes. Avoid breathing in the vapour.
Wear protective gloves provided when applying the product or when handling recently treated animals.
Wash splashes from the skin immediately with soap and plenty of water.
Wash hands and exposed skin before meals and after work.
4.6 Adverse reactions (frequency and seriousness)
Slightly irritant to the skin and mucous membranes.
4.7 Use during pregnancy, lactation or lay
Bayticol is safe to use in pregnant and lactating animals.
4.8 Interaction with other medicinal products and other forms of interaction
None known.
4.9 Amounts to be administered and administration route
Ascertain the weight of the animals to be treated.
Squeeze the required dose volume into the dosemeter (provided) and apply the contents along the back line of the animal from the front of the shoulder to the tail setting.
Treat at 14 day intervals according to tick pressure.
Control of ticks and biting lice
1 mg/kg b.w. of the active ingredient equivalent to 1 ml of the solution for every 10 kg bodyweight.
Control of Sucking lice and mange
2 mg/kg b.w. of the active ingredient equivalent to 2ml of the solution for every 10 kg bodyweight.
In cases of clinically severe mange a repeat treatment is necessary after 14 days.
Bayticol may be used in beef and dairy cattle including pregnant animals.
All animals in the herd should be treated. Bought-in-animals should also be treated and yarded for some hours before joining the herd.
4.10 Overdose (symptoms, emergency procedures, antidotes), if necessary
In trials 10 times the recommended dose rate (10 mg/kg b.w.) applied to calves did not cause any detectable side
effects.
Symptoms of poisoning:- Ataxia, dyspnoea, apathy.
Treat symptomatically. Gastric lavage or saline laxative may be used.
No data available on specific antidote.
4.11Withdrawal Period(s)
Animals must not be slaughtered for human consumption during treatment.
Animals must not be slaughtered for human consumption until 5 days after the last treatment.
Milk for human consumption may be taken only after 10 days following the last treatment.
5 PHARMACOLOGICAL or IMMUNOLOGICAL PROPERTIES
Pharmacotherapeutic group:
Ectoparasiticides for topical use, pyrethroids
ATCvet code:
QP53AC05
5.1 Pharmacodynamic properties
Flumethrin is an ectoparasticide of the synthetic pyrethroid group.
According to current knowledge the synthetic pyrethroids interfere with the sodium channel of nerve cell membranes,
resulting in a delay in repolarization of the nerve.
Alpha-cyano pyrethroids (type-II pyrethroids) like Flumethrin appear to be much more potent in this regard causing long-lasting trains of repetitive firing in nerve cells.
In studies on the structure-activity relationship of a number of pyrethroids, interference with receptors of a certain chiral conformation was noted thereby causing selective activity on ectoparasites.
No anti-cholinesterase activity was noted with these compounds.
Flumethrin was found to have an outstanding acaricidal activity.
6 PHARMACEUTICAL PARTICULARS
6.1 List of excipients
2-Octyldodecanol
Butylhydroxytoluene
Liquid paraffin
6.2 Incompatibilities
None known.
6.3 Shelf-life
Shelf life of the veterinary medicinal product as packaged for sale: 3 years.
Following withdrawal of the first dose, use remainder of the product within 9 months. Discard unused material.
6.4 Special precautions for storage
Do not freeze.
6.5 Nature and composition of immediate packaging
Container material: Polyethylene/polyamide bottles of litre.
Closure: Polypropylene screw closure, blue.
Contents: Viscous yellow-brown oil.
Dosemeter: Graduated polypropylene measuring cup with a polyethylene lid.
6.6 Special precautions for the disposal of unused veterinary medicinal products or waste materials
Toxic to bees and fish and other aquatic organisms.
Do not contaminate ponds, streams or other waterways with unused product or empty containers.
Any unused veterinary medicinal product or waste materials derived from such veterinary medicinal product should be disposed of in accordance with local requirements
7 MARKETING AUTHORISATION HOLDER
Bayer Limited,
Animal Health Division,
The Atrium,
Blackthorn Road,
Dublin 18
8 MARKETING AUTHORISATION NUMBER(S)
VPA 10021/010/001
9 DATE OF THE FIRST AUTHORISATION/RENEWAL OF THE AUTHORISATION
30th September 2009
Cattle Pour-ons
These should be applied along the length of the flattest part of the animal’s back, from the withers to the tail head.
In general, animals should not be treated when the hair is wet or if rain is anticipated within two hours of treatment. However, some products are waterproof and can be used on wet animals.
Areas of damaged skin should be avoided, as should areas contaminated with mud or manure
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